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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2755Erstellt: 24. Oktober 2026

Benzoyl Peroxide → 4-(Benzhydrylidene-amino)-3-bromomethyl-benzonitrile

https://huagongshe.com/de/reaction/2755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt4-(Benzhydrylidene-amino)-3-methyl-benzonitrileHCID 19350962—
LösungsmittelCarbon TetrachlorideHCID 5943—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(Benzhydrylidene-amino)-3-bromomethyl-benzonitrileHCID 1049968656,9%

Reaktionsschritte

To a solution of 4-(benzhydrylidene-amino)-3-methyl-benzonitrile (1.36 g, 4.27 mmol) in 40 mL of CCl4 is added N-bromosuccinimide (0.84 g, 4.7 mmol) and benzoyl peroxide (0.22 g, 0.64 mmol). The solution is heated to reflux for 16 h. The solution is cooled to ambient temperatures. The solution is diluted with CH2Cl2. The solution is washed with 1N NaOH and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude material is purified by column chromatography eluting with a gradient of 5% EtOAc/hexanes to 10% EtOAc/hexanes. The title compound (0.91 g, 2.43 mmol) is obtained as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731315
Quelldatensatzuspto-grants-1998_03
ORD IDord-d5d7a05761ee49b4bed0ffdf724b4bc7
Quellennotizuspto-grants-1998_03